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  1. Cat.No. Product Name Information
  2. GC16219 Chlorothiazide Carbonic anhydrase inhibitor Chlorothiazide Chemical Structure
  3. GC14505 Chlorothiazide Sodium diuretic and antihypertensive Chlorothiazide Sodium Chemical Structure
  4. GC30410 Chlorthal-dimethyl (Dimethyl tetrachloroterephthalate) Chlorthal-dimethyl (Dimethyl tetrachloroterephthalate) used as a pesticide intermediate. Chlorthal-dimethyl (Dimethyl tetrachloroterephthalate) Chemical Structure
  5. GC35681 Chlorthalidone A thiazide-like diuretic Chlorthalidone Chemical Structure
  6. GC31828 Chlorthenoxazine (Chlorethylbenzmethoxazone) Chlorthenoxazine (Chlorethylbenzmethoxazone) is a nonsteroidal anti-inflammatory drug. Chlorthenoxazine (Chlorethylbenzmethoxazone) Chemical Structure
  7. GC31655 Cholera toxin (choleragen) Cholera toxin (choleragen) (Choleragen), an AB(5)-subunit toxin, enters host cells by binding the ganglioside GM1 at the plasma membrane (PM) and travels retrograde through the trans-Golgi Network into the endoplasmic reticulum (ER). Cholera toxin (choleragen) Chemical Structure
  8. GC33554 Chromafenozide (ANS118) Chromafenozide (ANS118) (ANS118) is a lepidopteran insecticide; it is highly effective in controlling various lepidopteran pests. Chromafenozide (ANS118) Chemical Structure
  9. GC38650 Chromium picolinate Chromium picolinate (Chromium (III) picolinate) reduces insulin resistance and has the potential for type 2 diabetes mellitus. Chromium picolinate Chemical Structure
  10. GC11154 Chromocarb Vasoprotectant Chromocarb Chemical Structure
  11. GC43266 Chromomycin A3

    Chromomycin A3 is an anthraquinone antibiotic and antitumor agent isolated from S.

     Chromomycin A3 Chemical Structure
  12. GC38647 Chrysene Chrysene is a high molecular weight (HMW), polycyclic aromatic hydrocarbon (PAH) known for its recalcitrance and carcinogenic properties. Chrysene Chemical Structure
  13. GC35688 Chrysin 7-O-beta-gentiobioside Chrysin 7-O-beta-gentiobioside (Chrysin 7-O-β-gentiobioside) is the glycosylation product of Chrysin. Chrysin 7-O-beta-gentiobioside Chemical Structure
  14. GC31930 Chymase-IN-1 Chymase-IN-1 is a potent, selective, orally active, nonpeptide inhibitor of human mast cell chymase with an IC50 of 29 nM. Chymase-IN-1 Chemical Structure
  15. GC32031 Chymase-IN-2 Chymase-IN-2 is a chymase modulator which is useful in the treatment of inflammatory and serine protease mediated disorders. Chymase-IN-2 Chemical Structure
  16. GC31189 CI-943 ((±)-CI-943) CI-943 ((±)-CI-943) is a potential antipsychotic agent. CI-943 ((±)-CI-943) Chemical Structure
  17. GC30731 Cicloxilic acid (Cycloxilic acid) Cicloxilic acid (Cycloxilic acid) is a biologically active agent. Cicloxilic acid (Cycloxilic acid) Chemical Structure
  18. GC31119 CID 1375606 A GPR27 agonist CID 1375606 Chemical Structure
  19. GC30473 CID-797718 CID-797718 is a compound with unknown details. CID-797718 Chemical Structure
  20. GC35695 Cimifugin 4'-O-β-D-glucopyranoside Cimifugin 4'-O-β-D-glucopyranoside is a derivative of cimifugin. Cimifugin 4'-O-β-D-glucopyranoside Chemical Structure
  21. GC11798 Cinchonidine alkaloid Cinchonidine Chemical Structure
  22. GC10746 Cinchophen Analgesic drug Cinchophen Chemical Structure
  23. GC15247 Cinepazide vasodilator Cinepazide Chemical Structure
  24. GC16161 Cinepazide maleate Calcium channel inhibitor Cinepazide maleate Chemical Structure
  25. GC30225 Cinoctramide Cinoctramide is an intermediate of pharmaceutical synthesis. Cinoctramide Chemical Structure
  26. GC45896 CINPA1 A CAR antagonist CINPA1 Chemical Structure
  27. GC30868 Cinromide (trans-3-Bromo-N-ethylcinnamamide) Cinromide (trans-3-Bromo-N-ethylcinnamamide) is an anticonvulsant agent. Cinromide (trans-3-Bromo-N-ethylcinnamamide) Chemical Structure
  28. GC30709 Cipropride S enantiomer Cipropride (S enantiomer) is the S enantiomer of cipropride; cipropride is an antiemetic drug. Cipropride S enantiomer Chemical Structure
  29. GC32473 Ciraparantag (PER977) Ciraparantag (PER977) Chemical Structure
  30. GC33719 Citenamide (AY-15613) Citenamide (AY-15613) is an anticonvulsant. Citenamide (AY-15613) Chemical Structure
  31. GC30491 Citiolone Citiolone is a derivative of the amino acid cysteine, used in liver therapy. Citiolone Chemical Structure
  32. GC38754 Ciwujianoside A1 Ciwujianoside A1 is isolated from the Eleutherococcus senticosus leaf. Ciwujianoside A1 Chemical Structure
  33. GC31045 CL-275838 CL-275838 is a memory-enhancing agent, also with potent antidepressant activities. CL-275838 Chemical Structure
  34. GC16681 Clinafloxacin (AM1091) Clinafloxacin (AM 1091) is a potent and broad-spectrum fluoroquinolone antibiotic, has inhibitory activity against gram-positive, gram-negative bacterias, and anaerobic pathogens in vitro. Clinafloxacin (AM1091) Chemical Structure
  35. GC30425 Clofentezine Clofentezine, a growth inhibitor, has sublethal effects on life-table parameters of Tetranychus urticae Koch females. Clofentezine Chemical Structure
  36. GC30460 Cloquintocet-mexyl Cloquintocet-mexyl is a herbicide, used to control coarse annual grass of the family poaceae (gramineae). Cloquintocet-mexyl Chemical Structure
  37. GC31040 Clothixamide (Clotixamide) Clothixamide (Clotixamide) is a thiazide derivative. Clothixamide (Clotixamide) Chemical Structure
  38. GC35712 Cloxyfonac Cloxyfonac is a plant growth regulator and a chemical transformation product; Pesticide agent. Cloxyfonac Chemical Structure
  39. GC31931 Clozic (ICI 55897) Clozic (ICI 55897) is a potential anti-arthritic agent. Clozic (ICI 55897) Chemical Structure
  40. GC30562 CNT2 inhibitor-1 CNT2 inhibitor-1 is a potent concentrative nucleoside transporter 2 Inhibitor (CNT2), with an IC50 of 640 nM for hCNT2. CNT2 inhibitor-1 Chemical Structure
  41. GC30386 Cobalt phthalocyanine (Cobalt(II) phthalocyanine) Cobalt phthalocyanine (Cobalt(II) phthalocyanine) is a catalyst of redox reaction, catalyzes aerobic regenerations of aldehydes and ketones from aldoximes and ketoximes has been developed. Cobalt phthalocyanine (Cobalt(II) phthalocyanine) Chemical Structure
  42. GC30696 Codon readthrough inducer 1 Codon readthrough inducer 1, containing pyrimidine bases, shows good readthrough activity. Codon readthrough inducer 1 Chemical Structure
  43. GC43292 Coelenterazine h Coelenterazine is a luciferin, a light-emitting biomolecule that serves as a substrate for luciferases or as a constituent of photoproteins, including aequorin. Coelenterazine h Chemical Structure
  44. GC43293 Coenzyme A Coenzyme A (CoA) is an essential cofactor functioning as an acyl group carrier and carbonyl-activating group for the citric acid cycle and fatty acid metabolism. Coenzyme A Chemical Structure
  45. GC32441 Colestyramine (Cholestyramine resin) Colestyramine (Cholestyramine resin) (Colestyramine) is a bile acid binding resin and can inhibit intestinal bile acid absorption which results in the increasing bile acid synthesis from cholesterol. Colestyramine (Cholestyramine resin) Chemical Structure
  46. GC35721 Collagen proline hydroxylase inhibitor-1 Collagen proline hydroxylase inhibitor-1 is an antifibroproliferative agents. Collagen proline hydroxylase inhibitor-1 Chemical Structure
  47. GC16899 Coluracetam Nootropic agent of the racetam family Coluracetam Chemical Structure
  48. GC31846 Complement factor D-IN-1 Complement factor D-IN-1 is a potent and selective small-molecule reversible factor d inhibitor, with IC50s of 0.006 and 0.05 μM in FD Thioesterolytic Fluorescent Assay and a MAC Deposition Assay, respectively. Complement factor D-IN-1 Chemical Structure
  49. GC31604 Compound 2 Compound 2 is an active compound used for the research of metabolic bone diseases. Compound 2 Chemical Structure
  50. GC18058 Conduritol B epoxide β-glucosidase inhibitor Conduritol B epoxide Chemical Structure
  51. GC18071 CORM-3

    CORM-3 is a water-soluble tricarbonyl ruthenium chloride (II) complex, which can release CO rapidly and has anti-inflammatory.

     CORM-3 Chemical Structure
  52. GC34893 CORM-401 CORM-401 contains manganese (Mn) as a metal center, CORM-401 can release CO. CORM-401 Chemical Structure
  53. GC33781 Coumetarol (Dicumoxane) Coumetarol (Dicumoxane) (Dicumoxane) is a vitamin K antagonist. Coumetarol (Dicumoxane) Chemical Structure
  54. GC30575 CP 375 CP 375 is a Fe3+ chelating agent, with a log K1 value of 14.50. CP 375 Chemical Structure
  55. GC32262 CP-28888 (CP 28888-27) CP-28888 (CP 28888-27) is an interferon inducer, more potent in mice, but is less active in man and devoid of antirhinovirus effects. CP-28888 (CP 28888-27) Chemical Structure
  56. GC31598 CP-319340(free base) CP-319340 free base is a microsomal triglyceride transfer protein (MTP) inhibitor. CP-319340(free base) Chemical Structure
  57. GC14828 CPHPC CPHPC is a ligand for serum amyloid P component (SAP) and intends to inhibit and dissociate SAP binding to amyloid fibrils and tangles. CPHPC Chemical Structure
  58. GC10021 CPI-360 EZH2 inhibitor CPI-360 Chemical Structure
  59. GC38547 Crocetine dimethyl ester Crocetine dimethyl ester (Dimethylcrocetin) is found in the stigmas of saffron (Crocus sativus L. Crocetine dimethyl ester Chemical Structure
  60. GC30348 Cruzain-IN-1 Cruzain-IN-1 is a covalent and reversible Cruzain inhibitor, with an IC50 of 10 nM. Cruzain-IN-1 Chemical Structure
  61. GC32638 CS476 (NSC302998) CS476 (NSC302998) is a potent hypoglycaemic agent. CS476 (NSC302998) Chemical Structure
  62. GC34340 CSN5i-3 CSN5i-3 is a potent, selective and orally available inhibitor of CSN5/Jab1, and inhibits CSN-catalysed Cul1 deneddylation with an IC50 value of 5.8?nM. CSN5i-3 Chemical Structure
  63. GC35755 CTX-0294885 hydrochloride CTX-0294885 hydrochloride is a broad spectrum kinase inhibitor that can capture 235 kinases from MDA-MB-231 cells, and can capture all members of the AKT family. CTX-0294885 hydrochloride Chemical Structure
  64. GC17637 CTX0294885 Pan-kinase inhibitor CTX0294885 Chemical Structure
  65. GC30177 Cyantraniliprole (HGW-86) Cyantraniliprole (HGW-86)(HGW-86) is an insecticide of the ryanoid class; has activity against pests such as Diaphorina citri that have developed resistance to other classes insecticides. Cyantraniliprole (HGW-86) Chemical Structure
  66. GC30272 Cyantraniliprole D3 (HGW-86 D3) Cyantraniliprole D3 is the deuterium labeled Cyantraniliprole, which is an insecticide of the ryanoid class. Cyantraniliprole D3 (HGW-86 D3) Chemical Structure
  67. GC16309 Cyclamic acid artificial sweetening agent Cyclamic acid Chemical Structure
  68. GC12130 Cyclandelate Inhibitor of rat hepatic acycloenzyme A Cyclandelate Chemical Structure
  69. GC15048 Cyclic di-GMP

    second messenger

     Cyclic di-GMP Chemical Structure
  70. GC17795 Cyclocytidine HCl Ancitabine (hydrochloride) is an important antileukemia drugs. Cyclocytidine HCl Chemical Structure
  71. GC11328 Cyclosporine Cyclosporine (Cyclosporine A) is an immunosuppressant which binds to the cyclophilin and inhibits phosphatase activity of calcineurin with an IC50 of 5 nM. Cyclosporine Chemical Structure
  72. GC35786 Cyhalofop Cyhalofop (Cyhalofop acid), the primary metabolite of Cyhalofop-butyl in susceptible grasses, is the herbicidally active metabolite. Cyhalofop Chemical Structure
  73. GC16883 Cyromazine insecticide, acaricide Cyromazine Chemical Structure
  74. GC35821 D-Desthiobiotin D-Desthiobiotin is a biotin derivative used in affinity chromatography and protein chromatography, also can be used for protein and cell labeling, detection and isolation. D-Desthiobiotin Chemical Structure
  75. GC35879 D-Lin-MC3-DMA

    Dilinoleylmethyl-4-dimethylaminobutyrate (D-Lin-MC3-DMA) are potent siRNA delivery vehicles in vivo.

     D-Lin-MC3-DMA Chemical Structure
  76. GC11860 D-Luciferin

    D-luciferin is the natural substrate of firefly luciferase. 

     D-Luciferin Chemical Structure
  77. GC38905 D-Methionine sulfoxide hydrochloride D-methionine sulfoxide hydrochloride is the D-isomer of Methionine sulfoxide hydrochloride. D-Methionine sulfoxide hydrochloride Chemical Structure
  78. GC35887 D-myo-Inositol 1,4,5-trisphosphate hexapotassium salt D-myo-Inositol 1,4,5-trisphosphate hexapotassium salt is the hexapotassium salt of D-myo-Inositol 1,4,5-trisphosphate (1,4,5-IP3), which is a second messenger that stimulates the discharge of calcium from the endoplasmic reticulum. D-myo-Inositol 1,4,5-trisphosphate hexapotassium salt Chemical Structure
  79. GC43566 D-Pantothenic Acid (sodium salt) D-Pantothenic Acid (sodium salt) (Sodium pantothenate) is an essential trace nutrient that functions as the obligate precursor of coenzyme A (CoA). D-Pantothenic Acid (sodium salt) Chemical Structure
  80. GC32040 D18024 D18024 is a phthalazinonderivat antiallergic and antihistaminic activity. D18024 Chemical Structure
  81. GC31515 D5D-IN-326 D5D-IN-326 is a selective, orally active delta-5 desaturase (D5D) inhibitor, with IC50s of 72 and 22 nM for rat and human D5D in enzymic and cell-based assays, respectively, has no effect on D6D or D9D activity. D5D-IN-326 Chemical Structure
  82. GC34554 DAAO inhibitor-1 DAAO inhibitor-1 is a potent D-amino acid oxidase (DAAO) inhibitor with an IC50 of 0.12 μM. DAAO inhibitor-1 Chemical Structure
  83. GC35804 Daidzein diacetate Daidzein diacetate is a derivative of Daidzein that is a soy isoflavone. Daidzein diacetate Chemical Structure
  84. GC30114 Dansyl glutathione (DNS-glutathione) Dansyl glutathione (DNS-glutathione) is a trapping agent for the quantitative estimation and identification of reactive metabolites. Dansyl glutathione (DNS-glutathione) Chemical Structure
  85. GC38174 Dapagliflozin impurity Dapagliflozin impurity is an enantiomer of Dapagliflozin which is a sodium-glucose transporter 2 inhibitor. Dapagliflozin impurity Chemical Structure
  86. GC33555 Dazopride (AHR-5531) Dazopride (AHR-5531) is an antiemetic agent. Dazopride (AHR-5531) Chemical Structure
  87. GC38765 DB04760 analog 1 DB04760 analog 1 is an analogue of DB04760. DB04760 analog 1 Chemical Structure
  88. GC16795 DCA DCA is a metabolic regulator in cancer cells' mitochondria with anticancer activity. DCA inhibits PDHK, resulting in decreased lactic acid in the tumor microenvironment. DCA increases reactive oxygen species (ROS) generation and promotes cancer cell apoptosis. DCA also works as NKCC inhibitor. DCA Chemical Structure
  89. GC38126 Deacetyl Ganoderic Acid F Deacetyl Ganoderic Acid F is a 7-anostane triterpenoid from Ganoderma lucidum. Deacetyl Ganoderic Acid F Chemical Structure
  90. GC34425 Debutyldronedarone D7 (SR-35021 D7) Debutyldronedarone D7 (SR-35021 D7) Chemical Structure
  91. GC33093 Decoyinine (Angustmycin A) Decoyinine (Angustmycin A) Chemical Structure
  92. GC13554 Deferoxamine mesylate

    Deferoxamine mesylate is a drug that chelates iron by forming a stable complex that prevents the iron from entering into further chemical reactions, and is used for the treatment of chronic iron overload in patients with transfusion-dependent anemias.

     Deferoxamine mesylate Chemical Structure
  93. GC38407 Dehydroabietic acid A diterpene acid with diverse biological activities Dehydroabietic acid Chemical Structure
  94. GC34003 Dehydrocholic acid A synthetic bile acid Dehydrocholic acid Chemical Structure
  95. GC33896 Deloxolone Deloxolone has the potential for inflammatory, ischemic and proliferative diseases treatment. Deloxolone Chemical Structure
  96. GC38084 Demethoxydeacetoxypseudolaric acid B analog Demethoxydeacetoxypseudolaric acid B analog (Compound 13b) is semi-synthesized by efficient routines from Pseudolaric acid B. It has potent activities against HMEC-1, HL-60, A-549, MB-MDA-468, BEL-7402, HCT116, and Hela cells with IC50s ranging from 0.136 to 1.162 μM. Demethoxydeacetoxypseudolaric acid B analog Chemical Structure
  97. GC30327 Denatonium benzoate (THS-839) Denatonium benzoate (THS-839) (THS-839) is the most bitter chemical compound known,used as aversive agents (bitterants) to prevent inappropriate ingestion. Denatonium benzoate (THS-839) Chemical Structure
  98. GC32045 Deprodone propionate (RD20000) Deprodone propionate (RD20000) (RD20000) is a corticosteroid which is obtained by esterifying with propionic acid the 17-position of the prednisolone skeleton and deoxidating its 21-position. Deprodone propionate (RD20000) Chemical Structure
  99. GC35839 Derazantinib Racemate Derazantinib Racemate (ARQ-087 Racemate) is the racemate of Derazantinib. Derazantinib is an orally bioavailable, ATP competitive tyrosine kinase inhibitor; exhibits potent activity against FGFR1-3 chondrocytes with IC50s of 4.5, 1.8, and 4.5 nM, respectively. Derazantinib Racemate Chemical Structure
  100. GC30402 Desbutyl Lumefantrine D9 (Desbutyl-benflumetol D9) Desbutyl Lumefantrine D9 (Desbutyl-benflumetol D9) is the deuterium labeled euterium labeled, which is a metabolite of Lumefantrine. Desbutyl Lumefantrine D9 (Desbutyl-benflumetol D9) Chemical Structure
  101. GC35844 Desoximetasone A glucocorticoid Desoximetasone Chemical Structure

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